Gremlin gene expression in bovine retinal pericytes exposed to elevated glucose

• Published in: British journal of ophthalmology Vol. 89; no. 12; pp. 1638 - 1642
• Main Authors: Kane, R, Stevenson, L, Godson, C, Stitt, A W, O’Brien, C
• Format: Journal Article
• Language: English
• Published: BMA House, Tavistock Square, London, WC1H 9JR BMJ Publishing Group Ltd 01.12.2005; BMJ; BMJ Publishing Group LTD; Copyright 2005 British Journal of Ophthalmology
• Subjects: Animals; Base Sequence; Biological and medical sciences; BMP; bone morphogenetic protein; Bone Morphogenetic Proteins - antagonists & inhibitors; bovine retinal pericytes; BRPC; carbonyl cyanide m-chlorophenylhydrazone; Cattle; CCCP; Cells, Cultured; connective tissue growth factor; CTGF; DAN; Diabetes; Diabetes Mellitus, Experimental - metabolism; Diabetic retinopathy; Diabetic Retinopathy - metabolism; differential screening-selected gene aberrative in the neuroblastoma; Disease Models, Animal; Endothelium; EST; expressed sequence tag; Gene expression; Gene Expression Regulation - drug effects; glucose; Glucose - pharmacology; Humans; Intercellular Signaling Peptides and Proteins - genetics; Intercellular Signaling Peptides and Proteins - metabolism; Kinases; Laboratory Science - Extended Reports; Male; MAP-kinase; MAPK; Medical sciences; Mice; Mice, Inbred BALB C; Miscellaneous; Molecular Sequence Data; Ophthalmology; PAI-1; PDGF; Pericytes - drug effects; Pericytes - metabolism; Phosphorylation; PKC; plasminogen activator inhibitor-1; platelet derived growth factor; Polymerase chain reaction; protein kinase C; Proteins; reactive oxygen species; Retina; Retina - cytology; Retina - drug effects; Retina - metabolism; Reverse Transcriptase Polymerase Chain Reaction - methods; reverse transcription-polymerase chain reaction; ROS; RT-PCR; Smooth muscle; Species Specificity; TGFβ; transforming growth factor β; Vascular endothelial growth factor; VEGF; α smooth muscle actin; α-SMA; Pericyte; Vertebrata; Mammalia; Bovine; Animal; Retina; Artiodactyla; Glucose; Ophthalmology; Gene expression; Retinal; Ungulata
• ISSN: 0007-1161; 1468-2079
• DOI: 10.1136/bjo.2005.069591

Aim: To assess the influence of high extracellular glucose on the expression of the bone morphogenetic protein (BMP) antagonist, gremlin, in cultured bovine retinal pericytes (BRPC). Methods: BRPC were cultured under conditions of 5 mM and 30 mM d-glucose for 7 days and total RNA was isolated. Gremlin mRNA levels were correlated, by RT-PCR, with other genes implicated in the pathogenesis of diabetic retinopathy and the signalling pathways in high glucose induced gremlin expression were probed using physiological inhibitors. Gremlin expression was also examined in the retina of streptozotocin induced diabetic mice. Results: High glucose stimulated a striking increase in BRPC gremlin mRNA levels in parallel with increases in mRNA for the growth factors vascular endothelial growth factor (VEGF), transforming growth factor β (TGFβ), and connective tissue growth factor (CTGF) and changes in other genes including fibronectin and plasminogen activator inhibitor-1 (PAI-1). High glucose triggered gremlin expression was modulated by anti-TGFβ antibody, by the uncoupler of oxidative phosphorylation, CCCP, and by inhibition of MAP-kinase (MAPK) activation. Striking gremlin expression was observed in the outer retina of diabetic mice and also at the level of the vascular wall. Conclusions: Gremlin gene expression is induced in BRPC in response to elevated glucose and in the retina of the streptozotocin induced diabetic mouse. Its expression is modulated by hyperglycaemic induction of the MAPK, reactive oxygen species, and TGFβ pathways, all of which are reported to have a role in diabetic fibrotic disease. This implicates a role for gremlin in the pathogenesis of diabetic retinopathy.